ArticleBritish journal of pharmacology1993
Differential effects of acetylcholine, nitric oxide and levcromakalim on smooth muscle membrane potential and tone in the rabbit basilar artery.
Article in British journal of pharmacology, 1993. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.
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Who cites it
19 citing papers in PubMed, 82 citations in OpenAlex.
- Acute activation of endothelial AMPK surprisingly inhibits endothelium-dependent hyperpolarization-like relaxations in rat mesenteric arteries.British journal of pharmacology · 2019Article
- Smooth Muscle Ion Channels and Regulation of Vascular Tone in Resistance Arteries and Arterioles.Comprehensive Physiology · 2017Review
- Potassium Channels in Regulation of Vascular Smooth Muscle Contraction and Growth.Advances in pharmacology (San Diego, Calif.) · 2017Review
- Regulation of cellular communication by signaling microdomains in the blood vessel wall.Pharmacological reviews · 2014Review
- EDHF: spreading the influence of the endothelium.British journal of pharmacology · 2011Review
- NO and the vasculature: where does it come from and what does it do?Heart failure reviews · 2002Review
- Relaxation to authentic nitric oxide and SIN-1 in rat isolated mesenteric arteries: variable role for smooth muscle hyperpolarization.British journal of pharmacology · 2001Article
- Action of a NO donor on the excitation-contraction pathway activated by noradrenaline in rat superior mesenteric artery.The Journal of physiology · 2000Article
- Levcromakalim causes indirect endothelial hyperpolarization via a myo-endothelial pathway.British journal of pharmacology · 1999Article
- Effect of nitro-L-arginine on electrical and mechanical responses to acetylcholine in the superior mesenteric artery from stroke-prone hypertensive rat.British journal of pharmacology · 1999Article
- Acetylcholine-induced K+ currents in smooth muscle cells of intact rat small arteries.The Journal of physiology · 1997Article
- Endothelium-derived factors and hyperpolarization of the carotid artery of the guinea-pig.British journal of pharmacology · 1996Article
- Apamin-sensitive K+ channels mediate an endothelium-dependent hyperpolarization in rabbit mesenteric arteries.The Journal of physiology · 1995Article
- Nitric oxide hyperpolarizes rabbit mesenteric arteries via ATP-sensitive potassium channels.The Journal of physiology · 1995Article
- Substance P-induced relaxation and hyperpolarization in human cerebral arteries.British journal of pharmacology · 1995Article
- Multiple pathways underlying endothelium-dependent relaxation in the rabbit isolated femoral artery.British journal of pharmacology · 1995Article
- The relative importance of nitric oxide and nitric oxide-independent mechanisms in acetylcholine-evoked dilatation of the rat mesenteric bed.British journal of pharmacology · 1994Article
- Contribution of both nitric oxide and a change in membrane potential to acetylcholine-induced relaxation in the rat small mesenteric artery.British journal of pharmacology · 1994Article
- Nitric oxide-mediated inhibitory response of rat proximal colon: independence from changes in membrane potential.British journal of pharmacology · 1994Article
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Authors and funding
2 authors at 1 institution in 1 country.
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Abstract
1. Endothelium-dependent hyperpolarization of smooth muscle cells in isolated, pre-contracted segments of rabbit basilar artery in response to acetylcholine (100 microM) was abolished in the presence of glibenclamide (10 microM). 2. Acetylcholine-evoked relaxation was unaffected by either glibenclamide or 65 mM potassium chloride, indicating that the change in membrane potential did not form an essential component of relaxation and that high concentrations of potassium did not inhibit the release or action of endothelium-derived relaxing factor in this vessel. 3. Saturated solutions of nitric oxide (NO) gas in solution (150 microM), which evoked maximal relaxation of arterial segments pre-contracted and depolarized by noradrenaline (10-100 microM), did not alter the membrane potential of either unstimulated or depolarized smooth muscle cells. 4. The potassium channel opener levcromakalim, evoked concentration-dependent relaxation and hyperpolarization in pre-constricted smooth muscle cells. The threshold concentrations for hyperpolarization and relaxation, the EC50 values and the maximally effective concentration of levcromakalim (around 30 nM, 150 nM and 10 microM, respectively) were not significantly different, and both components of the response were inhibited by glibenclamide (10 microM), indicating a close coupling between the two responses. 5. In the presence of 65 mM potassium chloride, the hyperpolarization to levcromakalim was abolished, while a small relaxation (25 +/- 4%) persisted, indicating an additional mechanism for relaxation to this agent. 6. These results show that different mechanisms underlie the relaxant action of potassium channel openers, NO and endothelium-derived factors in cerebral arteries and provide further evidence that in the basilar artery, in contrast to some other vessels, endothelium-dependent hyperpolarization to acetylcholine is not important for smooth muscle relaxation.
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